反応式
[Cl:1]C1C=C(C(O)CNC(C)CC2C=CC3OC(C(O)=O)(C(O)=O)OC=3C=2)C=CC=1.COCCO.Cl.[CH3:36][O:37][CH2:38][CH2:39][O:40][C:41]([C:43]1([C:66]([O:68][CH2:69][CH2:70][O:71][CH3:72])=[O:67])[O:47][C:46]2[CH:48]=[CH:49][C:50]([CH2:52][CH:53]([NH:55][CH2:56][CH:57]([C:59]3[CH:64]=[CH:63][CH:62]=[C:61]([Cl:65])[CH:60]=3)[OH:58])[CH3:54])=[CH:51][C:45]=2[O:44]1)=[O:42]>CCOCC>[ClH:1].[CH3:36][O:37][CH2:38][CH2:39][O:40][C:41]([C:43]1([C:66]([O:68][CH2:69][CH2:70][O:71][CH3:72])=[O:67])[O:47][C:46]2[CH:48]=[CH:49][C:50]([CH2:52][CH:53]([NH:55][CH2:56][CH:57]([C:59]3[CH:64]=[CH:63][CH:62]=[C:61]([Cl:65])[CH:60]=3)[OH:58])[CH3:54])=[CH:51][C:45]=2[O:44]1)=[O:42]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 23 °C
実験手順
To a stirred mixture of 5-{2-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-propyl}-benzo[1,3]dioxole-2,2-dicarboxylic acid (1.0 g, 2.37 mmol), and 2-methoxy-1-ethanol (10 mL) was added excess HCl(g). The mixture became homogeneous and was stirred at 23° C. After 12 h, the solution was concentrated, and chromatographed on silica gel, eluting with CHCl3 /MeOH (1/0, then 40/1, 20/1 and 10/1) to give fractions containing 5-{2-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-propyl}-benzo[1,3]dioxole-2,2-dicarboxylic acid bis-(2-methoxy-ethyl) ester (Rf =0.37 (10/1 CHCl3 /MeOH)) as a viscous oil. This oil was dissolved in Et2O (10 mL) and HCl(g) was bubbled through the solution for 1 min. The resulting solution was evaporated to give 1.06 g (78%) of 5-{2-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-propyl}-benzo[1,3]dioxole-2,2-dicarboxylic acid bis-(2-methoxy-ethyl) ester hydrochloride salt as a white solid; 1H NMR (300 MHz, CDCl3): δ 1.33 (brm, 3H), 2.75-2.88 (brm, 1H), 3.10-3.30 (brm, 2H), 3.35 (s, 6H), 3.40-3.53 (brm 2H), 3.63-3.68 (complexm, 4H), 4.40-4.48 (brm, 4H), 5.40-5.50 (brd, 1H), 5.50-5.75 (brs, 1H), 6.70-6.91 (complex m, 4H), 7.18-7.38 (m, 2H), 7.43 (s, 1H), 8.60-8.85 (brs, 1H), 9.90-10.15 (brs, 1H); MS (ES) m/z (relative intensity): 538 (M+ -HCl, 100).
後処理
- concentrationthe solution was concentrated
- customchromatographed on silica gel
- washeluting with CHCl3 /MeOH (1/0
- custom40/1, 20/1 and 10/1) to give fractions
- customHCl(g) was bubbled through the solution for 1 min
- customThe resulting solution was evaporated
出典と根拠
- ORDレコード
- ord-2151a54f80034c1ea22a2a102fb01d8d
- 出典データセット
- uspto-grants-1999_06
- 特許番号
- US05914339
関連ノート
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